(Q56905828)

English

The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders

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scholarly article

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The CTLA4/CD28 gene region on chromosome 2q33 confers susceptibility to celiac disease in a way possibly distinct from that of type 1 diabetes and other chronic inflammatory disorders (English)

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type-1 diabetes

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Tommy Martinsson

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object named as

T Martinsson

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Staffan Nilsson

2

object named as

S Nilsson

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author name string

A T Naluai

1

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L Samuelsson

3

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A H Gudjónsdóttir

4

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H Ascher

5

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J Ek

6

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B Hallberg

7

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B Kristiansson

8

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O Nerman

10

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L M Sollid

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J Wahlström

12

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language of work or name

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publication date

October 2000

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Tissue Antigens

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56

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350-5

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4

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Molecular basis of celiac disease

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Increasing incidence of coeliac disease in Sweden

1 reference

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Increasing incidence of childhood coeliac disease in Sweden. Results of a national study

1 reference

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Epidemic of coeliac disease in Swedish children.

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HLA susceptibility genes in celiac disease: genetic mapping and role in pathogenesis

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An autosomal screen for genes that predispose to celiac disease in the western counties of Ireland

1 reference

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Genome search in celiac disease.

1 reference

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Linkage analysis of candidate regions for coeliac disease genes

1 reference

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A pedigree-based linkage study of coeliac disease: failure to replicate previous positive findings

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

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CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

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based on heuristic

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CTLA-4 gene polymorphism is associated with predisposition to coeliac disease

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

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Insulin-dependent diabetes mellitus (IDDM) is associated with CTLA4 polymorphisms in multiple ethnic groups

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

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The CTLA-4 gene region of chromosome 2q33 is linked to, and associated with, type 1 diabetes. Belgian Diabetes Registry

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

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Analysis of candidate genes for susceptibility to type I diabetes: a case-control and family-association study of genes on chromosome 2q31-35.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

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Non-HLA genes and the susceptibility to insulin dependent diabetes: the role of the CTLA-4 gene

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

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Association of CTLA-4 gene A-G polymorphism (IDDM12 locus) with acute-onset and insulin-depleted IDDM as well as autoimmune thyroid disease (Graves' disease and Hashimoto's thyroiditis) in the Japanese population

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

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CTLA4 gene haplotypes cannot protect from IDDM in the presence of high-risk HLA DQ8 or DQ2 alleles in German families.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

inferred from DOI database lookup

No major role for the CTLA-4 gene in the association of autoimmune thyroid disease with IDDM

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

inferred from DOI database lookup

No evidence for allelic association of a human CTLA-4 promoter polymorphism with autoimmune thyroid disease in either population-based case-control or family-based studies.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

inferred from DOI database lookup

CTLA-4 promoter variants in patients with Graves' disease and Hashimoto's thyroiditis.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

inferred from DOI database lookup

CTLA4 alanine-17 confers genetic susceptibility to Graves' disease and to type 1 diabetes mellitus.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

inferred from DOI database lookup

CTLA4 gene polymorphism confers susceptibility to Graves' disease in Japanese.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

inferred from DOI database lookup

A CTLA-4 gene polymorphism is associated with both Graves disease and autoimmune hypothyroidism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

inferred from DOI database lookup

CTLA4 codon 17 dimorphism in patients with rheumatoid arthritis

1 reference

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7 January 2021

based on heuristic

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The CTLA-4 gene is associated with multiple sclerosis.

1 reference

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7 January 2021

based on heuristic

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Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4

1 reference

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Loss of CTLA-4 leads to massive lymphoproliferation and fatal multiorgan tissue destruction, revealing a critical negative regulatory role of CTLA-4

1 reference

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7 January 2021

based on heuristic

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Blockage of T-cell costimulation inhibits T-cell action in celiac disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

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Revised criteria for diagnosis of coeliac disease. Report of Working Group of European Society of Paediatric Gastroenterology and Nutrition

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0039.2000.560407.X

7 January 2021

based on heuristic

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An Mse I RFLP in the human CTLA4 promotor.

1 reference

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An extended transmission/disequilibrium test (TDT) for multi-allele marker loci.

1 reference

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Duration of exposure to gluten and risk for autoimmune disorders in patients with celiac disease. SIGEP Study Group for Autoimmune Disorders in Celiac Disease

1 reference

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Celiac disease and autoimmune endocrinologic disorders

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A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34

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A comprehensive genetic map of the human genome based on 5,264 microsatellites

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10.1034/J.1399-0039.2000.560407.X

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